Evidence Details for GLIPR1L2


Gene Symbol: | GLIPR1L2 ( MGC39497 ) |
---|---|
Gene Full Name: | GLI pathogenesis-related 1 like 2 |
Band: | 12q21.2 |
Quick Links | Entrez ID:144321; OMIM: 610394; Uniprot ID:GRPL2_HUMAN; ENSEMBL ID: ENSG00000180481; HGNC ID: 28592 |
Relate to Another Database: | SFARIGene; denovo-db |


>GLIPR1L2|144321|nucleotide
ATGGAGGCCGCAAGGCCCTTCGCCCGGGAGTGGAGGGCCCAGTCCCTACCCCTGGCAGTAGGGGGCGTTTTGAAGCTGCGGCTCTGTGAGCTGTGGCTACTGCTA
CTGGGTTCTAGTTTGAACGCCAGATTTTTGCCAGACGAGGAGGACGTAGACTTTATCAACGAGTACGTGAACCTCCACAATGAGCTGCGGGGCGACGTCATTCCC
CGAGGGTCTAACTTGCGCTTCATGACTTGGGATGTAGCTTTATCACGGACTGCTAGAGCATGGGGAAAAAAATGTTTGTTTACGCATAATATTTATTTACAAGAT
GTACAAATGGTCCATCCTAAATTTTATGGTATTGGTGAAAATATGTGGGTCGGCCCTGAAAATGAATTTACTGCAAGTATTGCTATCAGAAGTTGGCATGCAGAG
AAGAAAATGTACAATTTTGAAAATGGCAGTTGCTCTGGAGACTGTTCTAATTATATTCAGCTTGTTTGGGACCACTCTTACAAAGTTGGTTGTGCTGTTACTCCA
TGTTCAAAAATTGGACATATTATACATGCAGCAATTTTCATATGCAACTATGCGCCAGGAGGAACACTGACGAGAAGACCTTATGAACCAGGAATATTTTGTACT
CGATGTGGCAGACGTGACAAATGCACAGATTTTCTATGCAGTAAGATAAAGAAAATAAACATGAAAAAAATGCATAATGGATTGGACAAGAAAAATAAGCGATTG
AACACTAGTTTTTTATGGTCATGTTAA
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ATGGAGGCCGCAAGGCCCTTCGCCCGGGAGTGGAGGGCCCAGTCCCTACCCCTGGCAGTAGGGGGCGTTTTGAAGCTGCGGCTCTGTGAGCTGTGGCTACTGCTA
CTGGGTTCTAGTTTGAACGCCAGATTTTTGCCAGACGAGGAGGACGTAGACTTTATCAACGAGTACGTGAACCTCCACAATGAGCTGCGGGGCGACGTCATTCCC
CGAGGGTCTAACTTGCGCTTCATGACTTGGGATGTAGCTTTATCACGGACTGCTAGAGCATGGGGAAAAAAATGTTTGTTTACGCATAATATTTATTTACAAGAT
GTACAAATGGTCCATCCTAAATTTTATGGTATTGGTGAAAATATGTGGGTCGGCCCTGAAAATGAATTTACTGCAAGTATTGCTATCAGAAGTTGGCATGCAGAG
AAGAAAATGTACAATTTTGAAAATGGCAGTTGCTCTGGAGACTGTTCTAATTATATTCAGCTTGTTTGGGACCACTCTTACAAAGTTGGTTGTGCTGTTACTCCA
TGTTCAAAAATTGGACATATTATACATGCAGCAATTTTCATATGCAACTATGCGCCAGGAGGAACACTGACGAGAAGACCTTATGAACCAGGAATATTTTGTACT
CGATGTGGCAGACGTGACAAATGCACAGATTTTCTATGCAGTAAGATAAAGAAAATAAACATGAAAAAAATGCATAATGGATTGGACAAGAAAAATAAGCGATTG
AACACTAGTTTTTTATGGTCATGTTAA
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>GLIPR1L2|144321|protein
MEAARPFAREWRAQSLPLAVGGVLKLRLCELWLLLLGSSLNARFLPDEEDVDFINEYVNLHNELRGDVIPRGSNLRFMTWDVALSRTARAWGKKCLFTHNIYLQD
VQMVHPKFYGIGENMWVGPENEFTASIAIRSWHAEKKMYNFENGSCSGDCSNYIQLVWDHSYKVGCAVTPCSKIGHIIHAAIFICNYAPGGTLTRRPYEPGIFCT
RCGRRDKCTDFLCSKIKKINMKKMHNGLDKKNKRLNTSFLWSC
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MEAARPFAREWRAQSLPLAVGGVLKLRLCELWLLLLGSSLNARFLPDEEDVDFINEYVNLHNELRGDVIPRGSNLRFMTWDVALSRTARAWGKKCLFTHNIYLQD
VQMVHPKFYGIGENMWVGPENEFTASIAIRSWHAEKKMYNFENGSCSGDCSNYIQLVWDHSYKVGCAVTPCSKIGHIIHAAIFICNYAPGGTLTRRPYEPGIFCT
RCGRRDKCTDFLCSKIKKINMKKMHNGLDKKNKRLNTSFLWSC
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Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default.
Evidences | Syndromic Gene | GWAS | CNV | Linkage | Association | Expression | NGS de novo | NGS Mosaic | NGS Other | Low-Scale Gene Studies | Total |
---|---|---|---|---|---|---|---|---|---|---|---|
Score (No. of Studies) | No | 0 (0) | 1 (2) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 2 (2) |






Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Szatmari, 2007 | Europe, North America | SNP microarray | ![]() | ![]() | ASD | 1491 | - | - | - | - | - | 0 |
Berkel, 2010 | Canada | SNP microarray | ![]() | ![]() | ASD | - | - | - | - | 396 | 5023 | 5419 |








Reference | Case Number | Family Number | de novo Number | Title |
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